Extended peptide-based inhibitors efficiently target the proteasome and reveal overlapping specificities of the catalytic beta-subunits.
第一作者:
B M,Kessler
第一单位:
Department of Pathology, Harvard Medical School, Boston, MA 02115, USA.
作者:
医学主题词
乙酰半胱氨酸(Acetylcysteine);催化域(Catalytic Domain);半胱氨酸内肽酶类(Cysteine Endopeptidases);半胱氨酸蛋白酶抑制剂(Cysteine Proteinase Inhibitors);酶抑制剂(Enzyme Inhibitors);人类(Humans);多酶复合物(Multienzyme Complexes);寡肽类(Oligopeptides);肽水解酶类(Peptide Hydrolases);肽类(Peptides);蛋白酶体内肽酶复合物(Proteasome Endopeptidase Complex);砜类(Sulfones)
DOI
10.1016/s1074-5521(01)00069-2
PMID
11564559
发布时间
2019-10-25
- 浏览49
Chemistry & biology
913-29页
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